Maria Brogaard is our state-authorised translator who has been with us for more than 15 years. Maria provides high-standard translations and proofreading of product information and all other documents in connection with regulatory procedures and pharmacovigilance in an environment where
In February 2019 Susanne Thiilborg, Ph.D.Pharm., began a position as Regulatory Affairs Manager with Billev Pharma. Susanne has more than 20 years’ experience within analytical chemistry from the pharmaceutical company Lundbeck. Susanne accounts for all possibilities and reviews the relevant
Trine Lorentzen, M.Sc. Pharm., filled the recently established post as QA Manager. Trine has several years of solid experience with Good Distribution Practice (GDP) and the function as Responsible Person. Are you facing an inspection? Are you struggling to keep
In June 2018 Karen Jensen, M.Sc. Pharm., joined our regulatory team. Karen and our regulatory team can assist you with both European and national initial MAAs or maintenance activities. Karen is a generous co-worker and has more than 16 years
In 2018 we celebrated Billev Pharma’s 40 years anniversary and also 3 times 10th anniversaries. Mette Skaarup Pedersen has been with us since 2008. Mette’s key area is proofreading and translation. Mette is highly respected among our clients for her
Er du den kollega vi leder efter? Så kan du læse mere om stillingen her: https://www.pharmadanmark.dk/da/Billev_Pharma_Pharmacovigilance
Celebrating 40 years of service to the pharmaceutical industry (1978-2018) – Simple solutions in a complex environment Read more about our services and our talented team here.
Har du erfaring med GMP, GDP og er du kvalificeret til at kunne fungere som QP for fx parallelimportører eller fremstillere af medicinsk cannabis. Måske drømmer du om nedsat tid? Så kontakt os. Vi tilbyder alsidige opgaver, en arbejdsplads med
Lisbeth Bonde Jensen, M.Sc. Pharmacy and Pg. Diploma in Pharmacovigilance, has been with us since April 2016. Lisbeth has more than 10 years of experience with Pharmacovigilance from the pharmaceutical industry. Are you interested in working with our highly skilled
Har du solid erfaring med Pharmacovigilance og søger du nye udfordringer? Så kontakt os. Vi tilbyder alsidige opgaver og fleksible arbejdsforhold. Vi forventer, at du hurtigt vil kunne arbejde selvstændigt med opgaverne.